Description
*Support Manufacturing/Process development with validation requirements of setting up the manufacturing facility.
*Ensure all requirements are laid out in protocols covering all aspects of equipment performance.
*Perform and manage all work in a safe manner and in compliance with local procedures/company standards and current health, safety and environment legislation.
*Ensure health & safety procedures are followed ie near miss accidents, Workstation assessment etc.
*Accountability for achieving validation timescales and highlighting potentially problematic processes.
*Help to design Factory acceptance test for complex equipment.
*Provide input to product validation requirements
*Setting key validation criteria and specifications.
5-10 years experience in all stages of equipment validation including production of documentation and working to project milestones.
Experience of setting up facility from scratch and validating line through to end of PQ.
Experience of manufacturing and/or engineering in previous roles.
Understanding of the requirements of Medical diagnostics manufacture.
Knowledgeable of ISO:13485 FDA 21 CFR 820 regulations
Hy-phen Limited is acting as an Employment Business in relation to this vacancy.
The Adecco Group UK & Ireland is an Equal Opportunities Employer.